A Review of Integrative Imputation for Multi-Omics Datasets

Multi-omics studies, which explore the interactions between multiple types of biological factors, have significant advantages over single-omics analysis for their ability to provide a more holistic view of biological processes, uncover the causal and functional mechanisms for complex diseases, and f...

Full description

Saved in:
Bibliographic Details
Published inFrontiers in genetics Vol. 11; p. 570255
Main Authors Song, Meng, Greenbaum, Jonathan, Luttrell, Joseph, Zhou, Weihua, Wu, Chong, Shen, Hui, Gong, Ping, Zhang, Chaoyang, Deng, Hong-Wen
Format Journal Article
LanguageEnglish
Published Switzerland Frontiers Media S.A 15.10.2020
Subjects
Online AccessGet full text

Cover

Loading…
More Information
Summary:Multi-omics studies, which explore the interactions between multiple types of biological factors, have significant advantages over single-omics analysis for their ability to provide a more holistic view of biological processes, uncover the causal and functional mechanisms for complex diseases, and facilitate new discoveries in precision medicine. However, omics datasets often contain missing values, and in multi-omics study designs it is common for individuals to be represented for some omics layers but not all. Since most statistical analyses cannot be applied directly to the incomplete datasets, imputation is typically performed to infer the missing values. Integrative imputation techniques which make use of the correlations and shared information among multi-omics datasets are expected to outperform approaches that rely on single-omics information alone, resulting in more accurate results for the subsequent downstream analyses. In this review, we provide an overview of the currently available imputation methods for handling missing values in bioinformatics data with an emphasis on multi-omics imputation. In addition, we also provide a perspective on how deep learning methods might be developed for the integrative imputation of multi-omics datasets.
Bibliography:ObjectType-Article-1
SourceType-Scholarly Journals-1
ObjectType-Feature-2
ObjectType-Review-3
content type line 23
Edited by: Mingyao Li, University of Pennsylvania, United States
Reviewed by: Wei-Min Chen, University of Virginia, United States; Dokyoon Kim, University of Pennsylvania, United States
This article was submitted to Statistical Genetics and Methodology, a section of the journal Frontiers in Genetics
ISSN:1664-8021
1664-8021
DOI:10.3389/fgene.2020.570255